Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Jihoon G Yoon

Showing results (11-20 of 37) with videos related to

Pageof 4
Sort By:
Nucleic Acids Research|January 20, 2026
A predictive framework for stop-loss variants with C-terminal extensionsJihoon G Yoon, Sojin Lee, Yoonjung Kim, et al.
Biomolecules & Therapeutics|September 6, 2019
Functional Characterization of Pharmcogenetic Variants of Human Cytochrome P450 2C9 in Korean PopulationsMyung-A Cho, Jihoon G Yoon, Vitchan Kim, et al.
Frontiers in Pediatrics|August 8, 2022
The extended clinical and genetic spectrum of <i>CTNNB1</i>-related neurodevelopmental disorderSeungbok Lee, Se Song Jang, Soojin Park, et al.
Brain Communications|September 21, 2023
Expansion of clinico-genetic spectrum of <i>PRDX3</i> disease: a literature review with two additional casesJaeso Cho, Jihoon G Yoon, Seungbok Lee, et al.
Annals of Laboratory Medicine|October 25, 2022
The First Korean Case of VEXAS Syndrome Caused by a <i>UBA1</i> Somatic VariantJihoon G Yoon, Seungbok Lee, Sheehyun Kim, et al.
Journal of Movement Disorders|July 8, 2024
Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay Masquerading as Charcot-Marie-Tooth Disease: A Case Study and Literature Review of Korean PatientsYongmoo Kim, Seungbok Lee, Jae So Cho, et al.
European Journal of Human Genetics : EJHG|February 2, 2024
Diagnostic uplift through the implementation of short tandem repeat analysis using exome sequencingJihoon G Yoon, Seungbok Lee, Jaeso Cho, et al.
Clinical and Experimental Pediatrics|December 21, 2023
Expanding association between BICD2 variants and brain malformations and associated lissencephalyJaeso Cho, Haeryung Kim, Seoungbok Lee, et al.
Pharmacogenetics and Genomics|November 9, 2020
A pilot study to investigate the utility of NAT2 genotype-guided isoniazid monotherapy regimens in NAT2 slow acetylatorsHyounggyoon Yoo, Sang Chun Ji, Joo-Youn Cho, et al.
Plos One|May 3, 2018
Machine learning-based diagnosis for disseminated intravascular coagulation (DIC): Development, external validation, and comparison to scoring systemsJihoon G Yoon, JoonNyung Heo, Minkyu Kim, et al.
Pageof 4

Showing results (11-20 of 37) with videos related to

Sort By:
Pageof 4
Nucleic Acids Research|January 20, 2026
A predictive framework for stop-loss variants with C-terminal extensionsJihoon G Yoon, Sojin Lee, Yoonjung Kim, et al.
Biomolecules & Therapeutics|September 6, 2019
Functional Characterization of Pharmcogenetic Variants of Human Cytochrome P450 2C9 in Korean PopulationsMyung-A Cho, Jihoon G Yoon, Vitchan Kim, et al.
Frontiers in Pediatrics|August 8, 2022
The extended clinical and genetic spectrum of <i>CTNNB1</i>-related neurodevelopmental disorderSeungbok Lee, Se Song Jang, Soojin Park, et al.
Brain Communications|September 21, 2023
Expansion of clinico-genetic spectrum of <i>PRDX3</i> disease: a literature review with two additional casesJaeso Cho, Jihoon G Yoon, Seungbok Lee, et al.
Annals of Laboratory Medicine|October 25, 2022
The First Korean Case of VEXAS Syndrome Caused by a <i>UBA1</i> Somatic VariantJihoon G Yoon, Seungbok Lee, Sheehyun Kim, et al.
Journal of Movement Disorders|July 8, 2024
Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay Masquerading as Charcot-Marie-Tooth Disease: A Case Study and Literature Review of Korean PatientsYongmoo Kim, Seungbok Lee, Jae So Cho, et al.
European Journal of Human Genetics : EJHG|February 2, 2024
Diagnostic uplift through the implementation of short tandem repeat analysis using exome sequencingJihoon G Yoon, Seungbok Lee, Jaeso Cho, et al.
Clinical and Experimental Pediatrics|December 21, 2023
Expanding association between BICD2 variants and brain malformations and associated lissencephalyJaeso Cho, Haeryung Kim, Seoungbok Lee, et al.
Pharmacogenetics and Genomics|November 9, 2020
A pilot study to investigate the utility of NAT2 genotype-guided isoniazid monotherapy regimens in NAT2 slow acetylatorsHyounggyoon Yoo, Sang Chun Ji, Joo-Youn Cho, et al.
Plos One|May 3, 2018
Machine learning-based diagnosis for disseminated intravascular coagulation (DIC): Development, external validation, and comparison to scoring systemsJihoon G Yoon, JoonNyung Heo, Minkyu Kim, et al.
Pageof 4